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CriticalFDAfda-F-0055-2025SALMONELLA CONTAMINATION

Chois Kimchi Company Gluten Free Gochujang Red Chili Paste, packaged 16oz plastic pouch with spout, keep refrigerated. UP 8 58878 00330 8...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
11
Recall Date
October 3, 2024
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0055-2025.

Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0055-2025.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Choi's Kimchi Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0055-2025.

Choi's Kimchi LLC

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Choi's Kimchi Llc Recall FAQ

Choi's Kimchi Llc is the subject of a food safety report: Chois Kimchi Company Gluten Free Gochujang Red Chili Paste, packaged 16oz plastic pouch with spout, keep refrigerated. UP 8 58878 00330 8.... The notice was published on October 3, 2024 by the U.S. Food and Drug Administration (FDA). Approximately 11 units are potentially affected.